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Where You From?


Guest DawterAod

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LJCurly9 Newbie

I'm from Rensselaer, Indiana...however, I'm currently a student at Butler University in Indianapolis.


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  • Replies 117
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Guest talsop

Evansville, Indiana

yllehs91 Apprentice

Southern TX...anyone from around the same area e-mail me! i'd really like to know someone near me that's going through the same thing...bcuz there are NO support groups where i am that i can find. (nearest is 2 hours away from me--corpus) and it'd be cool to meet people (if there are any besides me) that live close to me.

aim: ScoutNBoys1991

  • 1 month later...
Guest Bsecen

Hi everyone!!! I am from Orlando, Fl . :( Any relatives??? E-mail me!

Tiffany

minibabe Contributor
:D Hi, I was just recently diagnosed and I am from New York.....I live on Long Island. I am so glad that I found a message board.
pemmy Newbie

I'm from Glasgow in Scotland. I appear to be the only Celt on the board.

Great to hear about all the different places we come from. :)

  • 1 month later...
joe2008 Newbie

Downtown L.A.


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VegasCeliacBuckeye Collaborator

I live in Vegas.

Born in the U.K.

Raised in Dayton, Oh.

College at Ohio State (Columbus)

Graduate school in San Diego

Whew!

Vyse Newbie

Iowa here :)

Guest Viola

I'm in British Columbia, Canada. In the West Kootenay area, which is the southern part of the province. Only about four hours north of Spokan Washington.

Guest Leidenschaft

Hi all, this thread is very similar to our thread on Open Original Shared Link which asked to modify our signatures so that at a glance we could all know (on each and every post) where the other is from. Please have a glance through that thread! :)

Thanks!

sparkle2085 Newbie

Connecticut

  • 2 weeks later...
gabrielle Contributor
:D Amishtown, Pennsylvania
  • 2 weeks later...
Kels18 Newbie

Pittsburgh, Pennsylvania :rolleyes:

  • 4 weeks later...
teeta Newbie

INDIANA ( i thought if i did it in caps it might sound like more fun....... i dont think it worked)

jams Explorer

I'm from between Milwaukee & Madison Wisconsin!!

Guest GFLisa0405

Im from southeast michigan (halfway between detroit and ann arbor) tho i go to Central michigan in mt. pleasant

jenvan Collaborator

Hey! Shout out to the few from Indiana. I am in Indianapolis--the Ripple, for anyone who knows what that means :D

stef-the-kicking-cuty Enthusiast

Wow :o ! A lot of celiacs from PA here. Guys, we should meat. Maybe we could make a thread where we decide when and where we meat.

Oh, by the way, we're (my husband and I) moving. As of May 1st we will live in the Township (I first thought it's a municipality) of wheatfield :lol: .

kings-kid Newbie

Canada

wickedclown Newbie

brown city michigan..what what..throwin it up for the MI juggalos

  • 2 weeks later...
Guest Doct.Giggles

:P

I'm from Altmonte Springs, Florida!

Guest Doct.Giggles

:D I am from Altamonte Springs, Florida!!!!! :D

-Tiffany

  • 1 month later...
DragonQueen Explorer

Las Vegas, Nevada :lol:

selagirl Newbie

Im from Jerusalem, Israel :rolleyes:

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    • trents
      Certainly, it would b wise to have a gene test done if your physician is open to it as it would provide some more data to understand what's going on. But keep in mind that the genetic test for celiac disease cannot be used as to diagnose celiac disease, only to establish the potential to develop active celiac disease. About 40% of the general population possess one or both of the primary genes known to be associated with the development of active celiac disease but only about 1% of the population actually develop active celiac disease. So, the gene test is an effective "rule out" tool but not an effective diagnostic tool.
    • Roses8721
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      So you would be good with the diagnosis and not worry to check genetics etc etc? Appreciate your words!
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    • Scott Adams
      For those who will likely remain gluten-free for life anyway due to well-known symptoms they have when eating gluten, my general advice is to ignore any doctors who push to go through a gluten challenge to get a formal diagnosis--and this is especially true for those who have severe symptoms when they eat gluten. It can take months, or even years to recover from such a challenge, so why do this if you already know that gluten is the culprit and you won't be eating it anyway?  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS--but those in this group will usually have negative tests, or at best, elevated antibodies that don't reach the level of official positive. Unfortunately test results for celiac disease are not always definitive, and many errors can be made when doing an endoscopy for celiac disease, and they can happen in many ways, for example not collecting the samples in the right areas, not collecting enough samples, or not interpreting the results properly and giving a Marsh score.  Many biopsy results can also be borderline, where there may be certain damage that could be associated with celiac disease, but it just doesn't quite reach the level necessary to make a formal diagnosis. The same is true for blood test results. Over the last 10 years or so a new "Weak Positive" range has been created by many labs for antibody results, which can simply lead to confusion (some doctors apparently believe that this means the patient can decide if they want more testing or to go gluten-free). There is no "Weak Negative" category, for example. Many patients are not told to eat gluten daily, lots of it, for the 6-8 week period leading up to their blood test, nor asked whether or not they've been eating gluten. Some patients even report to their doctors that they've been gluten-free for weeks or months before their blood tests, yet their doctors incorrectly say nothing to them about how this can affect their test, and create false negative results. Many people are not routinely given a total IGA blood test when doing a blood screening, which can lead to false negative interpretations if the patient has low IGA. We've seen on this forum many times that some doctors who are not fully up on how interpret the blood test results can tell patients that the don't need to follow a gluten-free diet or get more testing because only 1 of the 2 or 3 tests done in their panel is positive (wrong!), and the other 1 or 2 tests are negative.  Dermatologists often don't know how to do a proper skin biopsy for dermatitis herpetiformis, and when they do it wrongly their patient will continue to suffer with terrible DH itching, and all the risks associated with celiac disease. For many, the DH rash is the only presentation of celiac disease. These patients may end up on strong prescriptions for life to control their itching which also may have many negative side effects, for example Dapsone. Unfortunately many people will continue to suffer needlessly and eat gluten due to these errors in performing or interpreting celiac disease tests, but luckily some will find out about non-celiac gluten sensitivity on their own and go gluten-free and recover from their symptoms. Consider yourself lucky if you've figured out that gluten is the source of your health issues, and you've gone gluten-free, because many people will never figure this out.    
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